Evidence map›Paper›PMID 42807637›Full record

ReviewFrontiers in cell and developmental biology2026

Immune-related biomarkers in liquid biopsy for cancer: emerging tools for non-invasive precision oncology.

Lai Wen, Xinhui Wang, Jinming Liu, Xinxin Pan, Yixin Zhang, Shuang Li, Mengying Tong, Yuankuan Jiang, Hewen Guan

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Lai Wen *Laboratory of Integrative Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Xinhui Wang *Laboratory of Integrative Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Jinming LiuLaboratory of Integrative Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Xinxin PanDepartment of Dermatology, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Yixin ZhangDepartment of Dermatology, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Shuang LiLaboratory of Integrative Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Mengying TongDepartment of Ultrasound, First Affiliated Hospital of Dalian Medical University, Dalian, China.
Yuankuan JiangDalian Dermatology Hospital, Dalian, China.
Hewen GuanLaboratory of Integrative Medicine, First Affiliated Hospital of Dalian Medical University, Dalian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liquid biopsy has emerged as a powerful non-invasive tool in precision oncology, providing real-time insights into tumor evolution, host immune responses, and dynamic changes in the tumor immune microenvironment. By enabling minimally invasive sampling, it can overcome several limitations of conventional tissue biopsy. This review summarizes the major biological sources and components of liquid biopsy, including circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), exosomes, and circulating immune cells, and discusses their value as dynamic indicators of interactions during cancer immunotherapy. Particular attention is given to immune-related biomarkers associated with immune checkpoints, immunosuppressive mechanisms, and immune escape, including circulating immune cell populations, and inflammatory cytokine profiles. We further examine their potential applications in predicting treatment response, monitoring immune-related adverse events, assessing minimal residual disease, and detecting acquired resistance. In addition, recent technological advances that are accelerating the clinical translation of liquid biopsy are highlighted, including multi-omics integration, microfluidic platforms. These approaches have improved the sensitivity, accuracy, and multidimensional characterization of tumor- and immune-derived biomarkers. Nevertheless, biological heterogeneity, limited assay standardization, and the lack of large-scale prospective validation studies continue to restrict widespread clinical implementation. Overall, immune-related biomarkers detected through liquid biopsy offer considerable potential for the longitudinal monitoring of the tumor immune microenvironment and may improve non-invasive cancer diagnosis, therapeutic monitoring, and personalized immunotherapy in the era of precision oncology.

Indexed as

circulating tumor DNAimmune-related biomarkersimmunotherapyliquid biopsytherapeutic monitoringtumor immune microenvironment

Identifiers

PMID42807637
PMCPMC13617286

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.